Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

-/TT/TTT | MAF: 0.44 (TT)

Chromosome 10: between 62389439 and 62389440 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 2510 sample genotypes.

Variant displays